Clinical Research Coor
About The Position
Coordinates daily operations of clinical research studies in assigned department(s). This includes but is not limited to overall clinic conduct, marketing, and data management of all clinical research activities in assigned department(s). Carries out supervisory responsibilities in accordance with policies and applicable laws. Responsibilities may include training new employees; assisting with planning, assigning, and directing work; addressing complaints and resolving problems. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to toxic or caustic chemicals and dangerous bodily fluids. The noise level in the work environment is usually moderate. Approximately 5-15% travel (often long-distance) is required.
Requirements
- Healthcare related training with current licensure/certification in their field OR Bachelor's degree from an accredited university with a major in the area of research being conducted.
- Ability to obtain certification as a Clinical Research Professional/Coordinator within two years from date of hire or upon eligibility.
Nice To Haves
- Certified Clinical Research Professional as defined by The Society of Clinical Research Associates or Certified Clinical Research Coordinator as defined by the Association of Clinical Research Professionals
Responsibilities
- Develop and maintain relationships with faculty members interested in or currently conducting clinical research.
- Develop and maintain relationships with assigned pharmaceutical, medical device, and other medical manufacturers considering clinical trials.
- Actively market the Clinical Research Institute.
- Facilitate IRB application and submission via Cayuse system.
- Facilitate ongoing and timely communication with the IRB via Cayuse system.
- Recruit and enroll human subject while protecting subjects and subjects’ rights.
- Maintain Study files/documents on all assigned studies.
- Facilitates data quality and integrity.
- Assist with development and management of research study budget.
- Assist faculty/staff with development of research protocols.
- Assist with clinical research education and training of volunteers, students, new employees.
- Attend affiliated clinical research meetings and professional meetings where research and compliance training may occur.
- Obtain SoCRA (CCRP) or ACRP (CCRC) certification when eligible.
- Maintain CPR certification.
- Maintain IATA training/certification.
- Maintain required institutional training to be able to participate in Clinical Research activities (i.e. CITI and HIPAA research training).
- Facilitates data quality and integrity.
- Participate in the Clinical Research call schedule rotation as needed.
- Obtain and maintain appropriate credentialing approval from University Medical Center Medical Staff office.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
